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Henian Cao

Showing results (1-10 of 66) with videos related to

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Journal of Human Genetics|July 12, 2002
Identification of single-nucleotide polymorphisms in the human LPIN1 geneHenian Cao, Robert A Hegele
Journal of Human Genetics|November 19, 2002
DNA polymorphisms in ITPA including basis of inosine triphosphatase deficiencyHenian Cao, Robert A Hegele
Journal of Human Genetics|August 16, 2002
Identification of polymorphisms in the human SHP1 geneHenian Cao, Robert A Hegele
Journal of Human Genetics|August 5, 2003
DNA polymorphisms of lipase related genesHenian Cao, Robert A Hegele
Journal of Human Genetics|February 1, 2003
DNA polymorphism and mutations in CPN1, including the genomic basis of carboxypeptidase N deficiencyHenian Cao, Robert A Hegele
Journal of Human Genetics|May 28, 2003
LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)Henian Cao, Robert A Hegele
Genomics|February 8, 2003
Genomic basis of mucopolysaccharidosis type IIID (MIM 252940) revealed by sequencing of GNS encoding N-acetylglucosamine-6-sulfataseAndrea Mok, Henian Cao, Robert A Hegele
Journal of Human Genetics|August 31, 2002
Functional promoter polymorphism in SREBP cleavage-activating protein (SCAP)Henian Cao, Brooke A Miskie, Robert A Hegele
Journal of Human Genetics|December 9, 2003
CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphismHenian Cao, Christina Williams, Monica Carter, et al.
Lipids in Health and Disease|February 2, 2008
Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemiaHenian Cao, Lindsay Alston, Jennifer Ruschman, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Journal of Human Genetics|July 12, 2002
Identification of single-nucleotide polymorphisms in the human LPIN1 geneHenian Cao, Robert A Hegele
Journal of Human Genetics|November 19, 2002
DNA polymorphisms in ITPA including basis of inosine triphosphatase deficiencyHenian Cao, Robert A Hegele
Journal of Human Genetics|August 16, 2002
Identification of polymorphisms in the human SHP1 geneHenian Cao, Robert A Hegele
Journal of Human Genetics|August 5, 2003
DNA polymorphisms of lipase related genesHenian Cao, Robert A Hegele
Journal of Human Genetics|February 1, 2003
DNA polymorphism and mutations in CPN1, including the genomic basis of carboxypeptidase N deficiencyHenian Cao, Robert A Hegele
Journal of Human Genetics|May 28, 2003
LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)Henian Cao, Robert A Hegele
Genomics|February 8, 2003
Genomic basis of mucopolysaccharidosis type IIID (MIM 252940) revealed by sequencing of GNS encoding N-acetylglucosamine-6-sulfataseAndrea Mok, Henian Cao, Robert A Hegele
Journal of Human Genetics|August 31, 2002
Functional promoter polymorphism in SREBP cleavage-activating protein (SCAP)Henian Cao, Brooke A Miskie, Robert A Hegele
Journal of Human Genetics|December 9, 2003
CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphismHenian Cao, Christina Williams, Monica Carter, et al.
Lipids in Health and Disease|February 2, 2008
Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemiaHenian Cao, Lindsay Alston, Jennifer Ruschman, et al.
Pageof 7